Thiele H, Berger M, Lenzner C, Kühn H, Thiele B J
Institute of Biochemistry, University Clinics Charité, Humboldt-University Berlin, Germany.
Eur J Biochem. 1998 Oct 1;257(1):62-8. doi: 10.1046/j.1432-1327.1998.2570062.x.
We have isolated genomic recombinants containing the complete gene coding for the rabbit translationally controlled tumor protein (TCTP), also known as histamine-releasing factor (HRF) P23. The gene is organized into five introns and six exons and its total length amounts to 3819 nucleotides. All intron/exon boundaries are in accordance with the GT/AG rule. Transcription of the gene generates two mRNAs of 843 and 1163 nucleotides differing in the length of their 3'-untranslated regions. They are formed by alternative polyadenylation. The transcription initiation site has been determined by comparison of sequences of the gene and several processed TCTP pseudogenes. The full-length 5'-untranslated region comprises 116 nucleotides and starts with an oligopyrimidine tract important for translational regulation. Additionally 1.2 kb of the 5'-flanking promoter region has been sequenced. The promoter contains a TATA box at -30 and potential binding sites for transcription factors such as stimulating protein 1 (Sp1), nuclear factor 1 (NF1), activator protein 1 (AP1), c-Ets1, cAMP-response element (CP2), myeloid-specific zinc finger protein 1 (MZF1) and others. For functional analysis 5'-flanking sequences up to -918 were fused to the chloramphenicol acetyltransferase (CAT) gene and tested using a rabbit aortic smooth-muscle cell line by cell transfection and CAT assays. The results confirm that the analyzed gene is the actively transcribed TCTP gene.
我们已经分离出了基因组重组体,其中包含编码兔翻译调控肿瘤蛋白(TCTP)的完整基因,该蛋白也被称为组胺释放因子(HRF)P23。该基因由五个内含子和六个外显子组成,全长为3819个核苷酸。所有内含子/外显子边界均符合GT/AG规则。该基因的转录产生了两种mRNA,分别为843和1163个核苷酸,它们的3'-非翻译区长度不同。它们是通过可变聚腺苷酸化形成的。转录起始位点已通过该基因与几个加工后的TCTP假基因的序列比较来确定。全长5'-非翻译区包含116个核苷酸,起始于对翻译调控很重要的寡嘧啶序列。此外,还对5'-侧翼启动子区域的1.2 kb进行了测序。该启动子在-30处含有一个TATA盒以及转录因子的潜在结合位点,如刺激蛋白1(Sp1)、核因子1(NF1)、激活蛋白1(AP1)、c-Ets-1、cAMP反应元件(CP2)、髓系特异性锌指蛋白1(MZF1)等。为了进行功能分析,将长达-918的5'-侧翼序列与氯霉素乙酰转移酶(CAT)基因融合,并通过细胞转染和CAT测定法在兔主动脉平滑肌细胞系中进行测试。结果证实所分析的基因是活跃转录的TCTP基因。